Arrow recalls VPS Rhythm ECG Accessory Pack with Johans Adapter (REF RHY-100-ECGJ) due to pouch labels potentially not showing lot numbers or expiration dates, which could affect catheter tip placement safety.
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Arrow is recalling a VPS Rhythm ECG Accessory Pack with Johans Adapter (REF RHY-100-ECGJ) because the product pouch may not clearly display the lot number or expiration date. This could lead to improper catheter tip placement if users cannot verify the product's date and batch.
The pouch label might not clearly show the lot number or expiration date. This could make it difficult for healthcare providers to confirm the product's date and batch, potentially leading to improper catheter tip placement if the product is used without verifying these details.
Healthcare professionals using the VPS Rhythm ECG Accessory Pack with Johans Adapter (REF RHY-100-ECGJ) for central venous catheter tip placement are affected. Those who use the product without verifying the lot number or expiration date are at slightly higher risk.
Check for the product name 'VPS Rhythm ECG Accessory Pack with Johans Adapter' and reference number RHY-100-ECGJ. Affected units have lot numbers 13F17A0287 or 13F17C0018.
Look for the lot number and expiration date on the pouch label to confirm if the product is affected.
The product pouch may not clearly display the lot number or expiration date, which could affect catheter tip placement safety.
Lot numbers 13F17A0287 and 13F17C0018 are affected.
No, but you should check the pouch label for the lot number and expiration date to ensure safe use.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2382-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2382-2018 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
